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O T Mueller

Showing results (11-20 of 25) with videos related to

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American Journal of Medical Genetics|August 14, 1995
Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothersO T Mueller, J K Hartsfield, M J Amar, et al.
Genomics|November 1, 1993
Correction of mucolipidosis III in vitro by gene transferM L Fowler, Y S Fan, O T Mueller, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1985
I-cell disease and pseudo-Hurler polydystrophy: heterozygote detection and characteristics of the altered N-acetyl-glucosamine-phosphotransferase in genetic variantsO T Mueller, L E Little, A L Miller, et al.
The Journal of Biological Chemistry|January 15, 1986
Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis IIIL E Little, O T Mueller, N K Honey, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1982
Mucolipidosis III is genetically heterogeneousN K Honey, O T Mueller, L E Little, et al.
American Journal of Medical Genetics|November 20, 1995
Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adultP R Papenhausen, O T Mueller, V P Johnson, et al.
Clinical Genetics|May 1, 1980
Adult GM1 gangliosidosis: clinical and biochemical studies on two patients and comparison to other patients called variant or adult GM1 gangliosidosisD A Wenger, M Sattler, O T Mueller, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1991
Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized resistance to thyroid hormoneS Ono, I D Schwartz, O T Mueller, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disordersO T Mueller, W M Henry, L L Haley, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 24, 2004
Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancyR A Quintero, O T Mueller, J M Martínez, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|August 14, 1995
Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothersO T Mueller, J K Hartsfield, M J Amar, et al.
Genomics|November 1, 1993
Correction of mucolipidosis III in vitro by gene transferM L Fowler, Y S Fan, O T Mueller, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 30, 1985
I-cell disease and pseudo-Hurler polydystrophy: heterozygote detection and characteristics of the altered N-acetyl-glucosamine-phosphotransferase in genetic variantsO T Mueller, L E Little, A L Miller, et al.
The Journal of Biological Chemistry|January 15, 1986
Heterogeneity of N-acetylglucosamine 1-phosphotransferase within mucolipidosis IIIL E Little, O T Mueller, N K Honey, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1982
Mucolipidosis III is genetically heterogeneousN K Honey, O T Mueller, L E Little, et al.
American Journal of Medical Genetics|November 20, 1995
Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adultP R Papenhausen, O T Mueller, V P Johnson, et al.
Clinical Genetics|May 1, 1980
Adult GM1 gangliosidosis: clinical and biochemical studies on two patients and comparison to other patients called variant or adult GM1 gangliosidosisD A Wenger, M Sattler, O T Mueller, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1991
Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized resistance to thyroid hormoneS Ono, I D Schwartz, O T Mueller, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disordersO T Mueller, W M Henry, L L Haley, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 24, 2004
Twin-twin transfusion syndrome in a dizygotic monochorionic-diamniotic twin pregnancyR A Quintero, O T Mueller, J M Martínez, et al.
Pageof 3